Investigating, planning and implementing medical product improvements and evaluate critical quality manufacturing processes that directly affect patient safety and product quality. Must successfully reduce defects of the clients devices and must aid in producing a better quality product more efficiently. Writing and executing physical and chemical test method protocols. Must adhere to quality policies like EU MDR, 21CFR820 set forth by FDA and respond to customer complaints, perform audits, developing test methods, validation etc. Must be willing to relocate and work anywhere in the US. Travel in the context of relocation may be required at least once or twice a year based on clients' needs.

Masters degree in Mechanical Engineering, Industrial Engineering, Biomedical Engineering or related is needed.